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ULTRA HYDRO FACIAL FOAM

Medically reviewed on Aug 31, 2018

Dosage form: liquid
Ingredients: GLYCERIN 0.015g in 1mL
Labeler: AMI Cosmetic Co.,Ltd.
NDC Code: 59535-1201

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Facts

glycerin


water, sodium laureth sulfate, sorbitol, sodium lauryl sulfate, cocamidopropyl betaine, cocamide dea, butylene glycol, propylene glycol, licorice root ext, platycodon grandiflorum root ext, centella asiatica ext, agaricus blazeil ext, rice bran ext, daffodil flower ext, oldenlandia diffusa ext, mentha arvensis leaf ext, sodium chloride phenoxyethanol, methylparaben, fragrance, gluceose, aloe barbadensis leaf juice powder, niacinamide, calcium panththenate, sodium ascorbyl phosphate, tocopheryl acetate, pyridoxine hci, chitin, disodium edta, citric acid, dextrin, maltodextrin, amylodextrin, silica


skin protectant



keep out of reach of the children

when cleansing with the mediclear facial foam, take adequate amount of the product to make foam with water, apply to face as if massaging and then wash it off with warm water


・Stop using the product when you have skin problems or the product disagrees with your skin.
・Stop using the product immediately and consult a dermatologist if you have redness, swelling, itching or irritation on the skin while or after using the product.
・If the product gets into the eyes, don't rub but rinse with water.
・Don't place the product in any place where it will be subjected to extremely high or low temperatures or direct sunlight.




for external use only

ULTRA HYDRO FACIAL FOAM 
glycerin liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59535-1201
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
GLYCERIN (GLYCERIN) GLYCERIN0.015 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
SODIUM LAURETH SULFATE 
SORBITOL 
NIACINAMIDE 
EDETATE DISODIUM 
Packaging
#Item CodePackage Description
1NDC:59535-1201-1250 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34708/31/2013
Labeler - AMI Cosmetic Co.,Ltd. (631055345)
Registrant - AMI Cosmetic Co.,Ltd. (631055345)
Establishment
NameAddressID/FEIOperations
GDKCOSMETICS Co., Ltd.557821946manufacture(59535-1201)

 
AMI Cosmetic Co.,Ltd.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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